124 related articles for article (PubMed ID: 38320813)
1. Wales Infants' and childreN's Genome Service (WINGS): providing rapid genetic diagnoses for unwell children.
Sloper E; Jezkova J; Thomas J; Dawson K; Halstead J; Gardner J; Burke K; Oruganti S; Calvert J; Evans J; Anderson S; Corrin S; Pottinger C; Murch O
Arch Dis Child; 2024 Apr; 109(5):409-413. PubMed ID: 38320813
[TBL] [Abstract][Full Text] [Related]
2. A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Kingsmore SF; Cakici JA; Clark MM; Gaughran M; Feddock M; Batalov S; Bainbridge MN; Carroll J; Caylor SA; Clarke C; Ding Y; Ellsworth K; Farnaes L; Hildreth A; Hobbs C; James K; Kint CI; Lenberg J; Nahas S; Prince L; Reyes I; Salz L; Sanford E; Schols P; Sweeney N; Tokita M; Veeraraghavan N; Watkins K; Wigby K; Wong T; Chowdhury S; Wright MS; Dimmock D;
Am J Hum Genet; 2019 Oct; 105(4):719-733. PubMed ID: 31564432
[TBL] [Abstract][Full Text] [Related]
3. Understanding access to genomics in an ethnically diverse south Florida population: A comparison of demographics in odyssey and rapid whole genome sequencing programs.
Hussain SB; Quittner AL; Brown M; Li-Rosi AM
J Genet Couns; 2020 Aug; 29(4):553-561. PubMed ID: 32277851
[TBL] [Abstract][Full Text] [Related]
4. Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of care.
Dimmock D; Caylor S; Waldman B; Benson W; Ashburner C; Carmichael JL; Carroll J; Cham E; Chowdhury S; Cleary J; D'Harlingue A; Doshi A; Ellsworth K; Galarreta CI; Hobbs C; Houtchens K; Hunt J; Joe P; Joseph M; Kaplan RH; Kingsmore SF; Knight J; Kochhar A; Kronick RG; Limon J; Martin M; Rauen KA; Schwarz A; Shankar SP; Spicer R; Rojas MA; Vargas-Shiraishi O; Wigby K; Zadeh N; Farnaes L
Am J Hum Genet; 2021 Jul; 108(7):1231-1238. PubMed ID: 34089648
[TBL] [Abstract][Full Text] [Related]
5. Rapid exome sequencing in critically ill children impacts acute and long-term management of patients and their families: A retrospective regional evaluation.
McDermott H; Sherlaw-Sturrock C; Baptista J; Hartles-Spencer L; Naik S
Eur J Med Genet; 2022 Sep; 65(9):104571. PubMed ID: 35842091
[TBL] [Abstract][Full Text] [Related]
6. Rapid Whole Genome Sequencing for Diagnosis of Single Locus Genetic Diseases in Critically Ill Children.
Owen MJ; Batalov S; Ellsworth KA; Wright M; Breeding S; Hugh K; Kingsmore SF; Ding Y
Methods Mol Biol; 2023; 2621():217-239. PubMed ID: 37041447
[TBL] [Abstract][Full Text] [Related]
7. Rapid Whole Genome Sequencing Diagnoses and Guides Treatment in Critically Ill Children in Belgium in Less than 40 Hours.
Lumaka A; Fasquelle C; Debray FG; Alkan S; Jacquinet A; Harvengt J; Boemer F; Mulder A; Vaessen S; Viellevoye R; Palmeira L; Charloteaux B; Brysse A; Bulk S; Rigo V; Bours V
Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835410
[TBL] [Abstract][Full Text] [Related]
8. Whole genome sequencing reveals that genetic conditions are frequent in intensively ill children.
French CE; Delon I; Dolling H; Sanchis-Juan A; Shamardina O; Mégy K; Abbs S; Austin T; Bowdin S; Branco RG; Firth H; ; ; Rowitch DH; Raymond FL
Intensive Care Med; 2019 May; 45(5):627-636. PubMed ID: 30847515
[TBL] [Abstract][Full Text] [Related]
9. Rapid exome sequencing: revolutionises the management of acutely unwell neonates.
Williamson SL; Rasanayagam CN; Glover KJ; Baptista J; Naik S; Satodia P; Gowda H
Eur J Pediatr; 2021 Dec; 180(12):3587-3591. PubMed ID: 34143244
[TBL] [Abstract][Full Text] [Related]
10. Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Farnaes L; Hildreth A; Sweeney NM; Clark MM; Chowdhury S; Nahas S; Cakici JA; Benson W; Kaplan RH; Kronick R; Bainbridge MN; Friedman J; Gold JJ; Ding Y; Veeraraghavan N; Dimmock D; Kingsmore SF
NPJ Genom Med; 2018; 3():10. PubMed ID: 29644095
[TBL] [Abstract][Full Text] [Related]
11. An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
Dimmock DP; Clark MM; Gaughran M; Cakici JA; Caylor SA; Clarke C; Feddock M; Chowdhury S; Salz L; Cheung C; Bird LM; Hobbs C; Wigby K; Farnaes L; Bloss CS; Kingsmore SF;
Am J Hum Genet; 2020 Nov; 107(5):942-952. PubMed ID: 33157007
[TBL] [Abstract][Full Text] [Related]
12. Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates.
Ayres S; Gallacher L; Stark Z; Brett GR
J Genet Couns; 2019 Apr; 28(2):273-282. PubMed ID: 30663825
[TBL] [Abstract][Full Text] [Related]
13. Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting.
Thompson L; Larson A; Salz L; Veith R; Tsai JP; Jayakar A; Chapman R; Gupta A; Kingsmore SF; Dimmock D; Bedrick A; Galindo MK; Casas K; Mohamed M; Straight L; Khan MA; Salyakina D
Front Pediatr; 2024; 12():1349519. PubMed ID: 38440187
[TBL] [Abstract][Full Text] [Related]
14. Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.
Sweeney NM; Nahas SA; Chowdhury S; Batalov S; Clark M; Caylor S; Cakici J; Nigro JJ; Ding Y; Veeraraghavan N; Hobbs C; Dimmock D; Kingsmore SF
NPJ Genom Med; 2021 Apr; 6(1):29. PubMed ID: 33888711
[TBL] [Abstract][Full Text] [Related]
15. Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project.
Wu B; Kang W; Wang Y; Zhuang D; Chen L; Li L; Su Y; Pan X; Wei Q; Tang Z; Li Y; Gao J; Cheng R; Zhou W; Wang Z; Qiu G; Wang J; Yang L; Zhang P; Zhao X; Wang Y; Gan M; Li G; Liu R; Ni Q; Xiao F; Yan K; Cao Y; Lu G; Lu Y; Wang H; Zhou W
Crit Care Med; 2021 Oct; 49(10):1674-1683. PubMed ID: 33935161
[TBL] [Abstract][Full Text] [Related]
16. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil.
Migliavacca MP; Sobreira J; Bermeo D; Gomes M; Alencar D; Sussuchi L; Souza CA; Silva JS; Kroll JE; Burger M; Guarischi-Sousa R; Villela D; Yamamoto GL; Milanezi F; Horigoshi N; Cesar RG; de Carvalho WB; Honjo RS; Bertola DR; Kim CA; de Souza L; Procianoy RS; Silveria RC; Rosenberg C; Giugliani R; Campana GA; Scapulatempo-Neto C; Sobreira N
Am J Med Genet A; 2024 Jun; 194(6):e63544. PubMed ID: 38258498
[TBL] [Abstract][Full Text] [Related]
17. Rapid Genome Sequencing Diagnosis in Pediatric Patients with Liver Dysfunction.
Bonser D; Malone Jenkins S; Palmquist R; Guthery S; Bonkowsky JL; Jaramillo C
J Pediatr; 2023 Sep; 260():113534. PubMed ID: 37269902
[TBL] [Abstract][Full Text] [Related]
18. RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Elliott AM; du Souich C; Lehman A; Guella I; Evans DM; Candido T; Tooman L; Armstrong L; Clarke L; Gibson W; Gill H; Lavoie PM; Lewis S; McKinnon ML; Nikkel SM; Patel M; Solimano A; Synnes A; Ting J; van Allen M; Christilaw J; Farrer MJ; Friedman JM; Osiovich H
Eur J Pediatr; 2019 Aug; 178(8):1207-1218. PubMed ID: 31172278
[TBL] [Abstract][Full Text] [Related]
19. Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States.
Diaby V; Babcock A; Huang Y; Moussa RK; Espinal PS; Janvier M; Soler D; Gupta A; Jayakar P; Diaz-Barbosa M; Totapally B; Sasaki J; Jayakar A; Salyakina D
Pharmacogenomics J; 2022 Jul; 22(4):223-229. PubMed ID: 35436997
[TBL] [Abstract][Full Text] [Related]
20. Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Willig LK; Petrikin JE; Smith LD; Saunders CJ; Thiffault I; Miller NA; Soden SE; Cakici JA; Herd SM; Twist G; Noll A; Creed M; Alba PM; Carpenter SL; Clements MA; Fischer RT; Hays JA; Kilbride H; McDonough RJ; Rosterman JL; Tsai SL; Zellmer L; Farrow EG; Kingsmore SF
Lancet Respir Med; 2015 May; 3(5):377-87. PubMed ID: 25937001
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
